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Pharmacological perturbation of CDK9 using selective CDK9 inhibition or degradation
Cyclin dependent kinase 9 (CDK9), a key regulator of transcriptional elongation, is a promising target for cancer therapy, particularly for cancers driven by transcriptional dysregulation. Here, we report the characterization of NVP-2 (3), a selective ATP-competitive CDK9 inhibitor; and THAL-SNS-032...
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| Udgivet i: | Nat Chem Biol |
|---|---|
| Main Authors: | , , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
2017
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5912898/ https://ncbi.nlm.nih.gov/pubmed/29251720 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nchembio.2538 |
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